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Eur J Mass Spectrom (Chichester) ; 10(5): 657-64, 2004.
Article in English | MEDLINE | ID: mdl-15531799

ABSTRACT

Duchenne muscular dystrophy (DMD) is a neuromuscular disease linked to the lack of the dystrophin, a submembrane protein, leading to muscle weakness and associated with a defect of the lipid metabolism. A study of the fatty acid composition of glycerophosphatidylcholines by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-ToF-MS) and tandem mass spectrometry (MS/MS) enabled us to characterize a change of the lipid composition of dystrophic cells at the time of the differentiation. This modification has been used as a marker to identify with profiling and imaging MALDI-ToF MS regenerating areas in sections of an mdx mouse leg muscle. It is the first time that such a slight change in fatty acid composition has been observed directly on tissue slices using mass spectrometry. This approach will be useful in monitoring the treatment of muscular regeneration.


Subject(s)
Glycerylphosphorylcholine/analysis , Muscle, Skeletal/chemistry , Muscular Dystrophy, Duchenne , Phosphatidylethanolamines/analysis , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods , Animals , Biomarkers/analysis , Cell Membrane/chemistry , Cell Membrane/metabolism , Cells, Cultured , Disease Models, Animal , Fatty Acids/analysis , Glycerylphosphorylcholine/metabolism , Mice , Mice, Inbred C57BL , Mice, Inbred mdx , Muscle, Skeletal/metabolism , Muscular Dystrophy, Duchenne/metabolism , Myoblasts/chemistry , Myoblasts/metabolism , Phosphatidylethanolamines/metabolism
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